Abstract
Surgery for congenitally corrected transposition of the great arteries (ccTGA) has evolved overtime. Anatomical repair of ccTGA is now performed with quite satisfactory outcomes in children. The double switch operation has become the preferred surgical procedure in selected cases. Nevertheless, a number of patients with ccTGA still require physiological repair due to complex cardiac associations or impaired systemic ventricular function. This chapter outlines the mechanisms of right ventricular failure in ccTGA. Several “old techniques of repair” were abandoned. The introduction of PA banding has reduced the occurrence of tricuspid regurgitation and has allowed, in some cases, anatomical repair after proper LV retraining. The indications for TV repair and replacement, the place of the Fontan operation or heart transplantation are discussed. The decision to proceed with physiologic versus anatomic repair and the timing of operation is individualized.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
References
Ferencz C, Rubin JD, McCarter RJ, et al. Congenital heart disease: prevalence at live birth. The Baltimore-Washington infant study. Am J Epidemiol. 1985;121:31–6.
Losekoot TG, Becker AE. Discordant atrioventricular connexion and congenitally corrected transposition. In: Anderson RH, MacCartney FJ, Shinebourne EA, Tynan A, editors. Paediatric cardiology. Edinburgh: Churchill Livingstone; 1987. p. 867–88.
Becker AE, Anderson RH. Atrioventricular discordance in pathology of congenital heart disease. London: Butterworth; 1981. p. 225–40.
Freedom RM, Benson LN, Smallhorn JF. Congenitally transposition of the great arteries. In: Moller JH, Neal WA, editors. Fetal, neonatal and infantcardiac disease. Norwalk: Appleton and Lange; 1989. p. 555–70.
Langley SM, Winlaw DS, Stumper O, et al. Midterm results after restoration of the morphologically left ventricle to the systemic circulation in patients with congenitally corrected transposition of the great arteries. J Thorac Cardiovasc Surg. 2003;125:1229–41.
Anderson KR, Danielson GK, McGoon DW, et al. Ebstein’s anomaly of the left-sided tricuspid valve. Pathological anatomy of the valvular malformation. Circulation. 1978;58:87–91.
Anderson RH, Becker AE, Arnold R, et al. The conducting tissues in congenitally corrected transposition. Circulation. 1974;50:911–23.
De Leval MR, Basto P, Stark J, et al. Surgical technique to reduce the risks of heart block following closure of ventricular septal defect in atrioventricular discordance. J Thorac Cardiovasc Surg. 1979;78:515–26.
Imai Y. Double-switch operation for congenitally corrected transposition. Adv Card Surg. 1997;9:65–86.
Prieto LR, Hordof AJ, Secic M, et al. Progressive tricuspid valve disease in patients with congenitally corrected transposition of the great arteries. Circulation. 1998;98:997–1005.
Beauchesne LM, Warnes CA, Connolly HM, et al. Outcome of the unoperated adult who presents with congenitally corrected transposition of the great arteries. J Am Coll Cardiol. 2002;40:285–90.
Warnes CA. The adult with congenital heart disease: born to be bad? J Am Coll Cardiol. 2005;46:1–8.
Mongeon FP, Connolly HM, Dearani JA, Li Z, Warnes CA. Congenitally corrected transposition of the great arteries ventricular function at the time of systemic atrioventricular valve replacement predicts long-term ventricular function. J Am Coll Cardiol. 2011;57:2008–17.
Dearani JA, Said SM, Burkhart HM, Pike RB, O’Leary PW, Cetta F. Strategies for tricuspid re-repair in Ebstein malformation using the cone technique. Ann Thorac Surg. 2013;96(1):202–8.
Hraska V, Duncan B, Mayer Jr JE, et al. Long-term outcome of surgically treated patients with corrected transposition of the great arteries. J Thorac Cardiovasc Surg. 2005;129:182–91.
Termignon JL, Leca F, Vouhe PR, et al. “Classic” repair of congenitally corrected transposition and ventricular septal defect. Ann Thorac Surg. 1996;62:199–206.
Metton O, Gaudin R, Ou P, et al. Early prophylactic pulmonary artery banding in isolated congenitally corrected transposition of the great arteries. Eur J Cardiothorac Surg. 2010;38(6):728–34.
Jahangiri M, Redington AN, Elliott MJ, et al. A case for anatomic correction in atrioventricular discordance? Effects of surgery on tricuspid valve function. J Thorac Cardiovasc Surg. 2001;121:1040–5.
Baslaim G. Modification of Trusler’s formula for the pulmonary artery banding. Heart Lung Circ. 2009;18(5):353–7.
Albus RA, Trusler GA, Izukawa T, Williams W. Pulmonary artery banding. J Thorac Cardiovasc Surg. 1984;88:645–53.
Trusler GA, Mustard WT. A method of banding the pulmonary artery for large isolated ventricular septal defect with and without transposition of the great arteries. Ann Thorac Surg. 1972;13:351–5.
Corno AF, Bonnet D, Sekarski N, Sidi D, Vouhé P, von Segesser LK. Remote control of pulmonary blood flow: initial clinical experience. J Thorac Cardiovasc Surg. 2003;126(6):1775–80.
Graham Jr TP, Bernard YD, Mellen BG, et al. Long-term outcome in congenitally corrected transposition of the great arteries: a multi-institutional study. J Am Coll Cardiol. 2000;36:255–61.
Acar P, Sidi D, Bonnet D, et al. Maintaining tricuspid valve competence in double discordance: a challenge for the pediatric cardiologist. Heart. 1998;80:479–83.
Tulevski II, Zijta FM, Smeijers AS, et al. Regional and global right ventricular dysfunction in asymptomatic or minimally symptomatic patients with congenitally corrected transposition. Cardiol Young. 2004;14:168–73.
Espinola-Zavaleta N, Erick AE, Attie F, et al. Right ventricular function and ventricular perfusion defects in adults with congenitally corrected transposition: correlation of echocardiography and nuclear medicine. Cardiol Young. 2004;14:174–81.
Gregoric ID, Kosir R, Smart FW, et al. Left ventricular assist device implantation in a patient with congenitally corrected transposition of the great arteries. Tex Heart Inst J. 2005;32:567–9.
Sue SH, Wei J, Chuang YC, et al. Cardiac transplantation for congenitally corrected transposition of the great arteries: a case report. Transplant Proc. 2008;40(8):2844–5.
Alghamdi AA, McCrindle BW, Van Arsdell GS. Physiologic versus anatomic repair of congenitally corrected transposition of the great arteries: meta-analysis of individual patient data. Ann Thorac Surg. 2006;81:1529–35.
Van Son JA, Danielson GK, Huhta JC, et al. Late results of systemic atrioventricular valve replacement in corrected transposition. J Thorac Cardiovasc Surg. 1995;109:642–52.
Rutledge JM, Nihill MR, Fraser CD, et al. Outcome of 121 patients with congenitally corrected transposition of the great arteries. Pediatr Cardiol. 2002;23:137–45.
Lundstrom U, Bull C, Wyse RK, et al. The natural and “unnatural” history of congenitally corrected transposition. Am J Cardiol. 1990;65:1222–9.
Metcalfe J, Somerville J. Surgical repair of lesions associated with corrected transposition: late results. Br Heart J. 1983;50:476–82.
McGrath LB, Kirklin JW, Blackstone EH, et al. Death and other events after cardiac repair in discordant atrioventricular connection. J Thorac Cardiovasc Surg. 1985;90:711–28.
Sano T, Riesenfeld T, Karl TR, et al. Intermediate-term outcome after intracardiac repair of associated cardiac defects in patients with atrioventricular and ventriculoarterial discordance. Circulation. 1995;92(9 suppl):II-272–8.
Scherptong RW, Vliegen HW, Winter MM, et al. Tricuspid valve surgery in adults with a dysfunctional systemic right ventricle: repair or replace? Circulation. 2009;119:1467–72.
Warnes CA. Transposition of the great arteries. Circulation. 2006;114:2699–709.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2016 Springer International Publishing Switzerland
About this chapter
Cite this chapter
Said, S.M., Dearani, J.A. (2016). Physiologic Repair of Congenitally Corrected Transposition of the Great Arteries. In: Lacour-Gayet, F., Bove, E., Hraška, V., Morell, V., Spray, T. (eds) Surgery of Conotruncal Anomalies. Springer, Cham. https://doi.org/10.1007/978-3-319-23057-3_29
Download citation
DOI: https://doi.org/10.1007/978-3-319-23057-3_29
Published:
Publisher Name: Springer, Cham
Print ISBN: 978-3-319-23056-6
Online ISBN: 978-3-319-23057-3
eBook Packages: MedicineMedicine (R0)